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34045

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Azaconazole

PESTANAL®, analytical standard

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Synonym(s):
1-[2-(2,4-Dichlorophenyl)-1,3-dioxolan-2-ylmethyl]-1H-1,2,4-triazole
Empirical Formula (Hill Notation):
C12H11Cl2N3O2
CAS Number:
Molecular Weight:
300.14
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

Clc1ccc(c(Cl)c1)C3(Cn2cncn2)OCCO3

InChI

1S/C12H11Cl2N3O2/c13-9-1-2-10(11(14)5-9)12(18-3-4-19-12)6-17-8-15-7-16-17/h1-2,5,7-8H,3-4,6H2

InChI key

AKNQMEBLVAMSNZ-UHFFFAOYSA-N

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This Item
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Azaconazole PESTANAL®, analytical standard

34045

Azaconazole

Prothioconazole-desthio PESTANAL®, analytical standard

32429

Prothioconazole-desthio

Prothioconazole PESTANAL®, analytical standard

34232

Prothioconazole

Bromuconazole PESTANAL®, analytical standard, mixture of diastereomers

31644

Bromuconazole

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

grade

analytical standard

grade

analytical standard

grade

analytical standard

grade

analytical standard

product line

PESTANAL®

product line

PESTANAL®

product line

PESTANAL®

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

shelf life

limited shelf life, expiry date on the label

shelf life

limited shelf life, expiry date on the label

shelf life

limited shelf life, expiry date on the label

application(s)

agriculture
environmental

application(s)

agriculture
environmental

application(s)

agriculture
environmental

application(s)

agriculture
environmental

General description

Azaconazole has been used as an internal standard in the determination of propiconazole, a fungistatic agent in white spruce, using gas chromatography/mass spectrometry (GC/MS).

Application

Azaconazole, is an agricultural fungicide, which shows activity against wood destroying fungi and sapstain fungi. It can also play the role of a disinfectant in mushroom cultivation and in the storage of fruits and vegetables.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


Certificates of Analysis (COA)

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G O Rankin et al.
Toxicology, 34(1), 1-11 (1985-01-01)
Azaconazole is an experimental agricultural fungicide which has shown promise for use in controlling powdery mildew on crops and bean rust. This study examined the nephrotoxic potential of a single intraperitoneal azaconazole injection (0.4 or 0.6 mmol/kg) or daily azaconazole
Roberts RT and Hutson HD
Metabolic Pathways of Agrochemicals: Herbicides and plant growth regulators; (1998)
Interaction of azole derivatives with cytochrome P-450 isozymes in yeast, fungi, plants and mammalian cells.
Bossche VH, et al.
Pest Management Science, 21.4, 289-306 (1987)
Raman microscopy for the quantitation of propiconazole in white spruce
Kurti E, et al.
Wood Science and Technology, 39.8, 618-629 (2005)
Bryce E Mansfield et al.
PLoS pathogens, 6(9), e1001126-e1001126 (2010-10-14)
Despite the wealth of knowledge regarding the mechanisms of action and the mechanisms of resistance to azole antifungals, very little is known about how the azoles are imported into pathogenic fungal cells. Here the in-vitro accumulation and import of Fluconazole

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